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Biotechnology Project Manager Jobs in Riverside, CA

Crane Co.

Project Engineer

Jurupa Valley, CA · On-site

Time management** -- Ability to prioritize tasks and manage multiple projects.**Interpersonal ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · On-site

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · Hybrid

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Stark Pharma Solutions Inc

QC Scientist

Irvine, CA · On-site

... Project Management, and IT, with a focus on delivering tailored solutions that drive growth ... biotech environment. Key Responsibilities * Perform hands-on HPLC and dissolution testing for drug ...

Zymo Research

Campaign Manager

Tustin, CA · On-site

$85K - $105K/yr

Your strong project management and tactical marketing skills will be essential in achieving ... Knowledge of biotechnology or life sciences is a plus. Education and Experience: * Minimum of 5 ...

Valid8 Financial, Inc.

Campaign Manager

Tustin, CA · On-site

$85K - $105K/yr

... project management tools. * Excellent communication and interpersonal skills. * Self-starter with the ability to independently lead campaigns from briefing to execution. * Knowledge of biotechnology ...

Zymo Research Corporation

Campaign Manager

Tustin, CA · On-site

$85K - $105K/yr

... project management tools. * Excellent communication and interpersonal skills. * Self-starter with the ability to independently lead campaigns from briefing to execution. * Knowledge of biotechnology ...

Zymo Research Corporation

Campaign Manager

Tustin, CA

$85K - $105K/yr

... project management tools. * Excellent communication and interpersonal skills. * Self-starter with the ability to independently lead campaigns from briefing to execution. * Knowledge of biotechnology ...

Zymo Research Corporation

Campaign Manager

Tustin, CA · On-site

$85K - $105K/yr

... project management tools. * Excellent communication and interpersonal skills. * Self-starter with the ability to independently lead campaigns from briefing to execution. * Knowledge of biotechnology ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

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Biotechnology Project Manager information

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$48

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How much do biotechnology project manager jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotechnology project manager in Riverside, CA is $48.24, according to ZipRecruiter salary data. Most workers in this role earn between $41.88 and $52.93 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Riverside, CA?

For Biotechnology Project Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Riverside, CA look for?

The top searched job categories for Biotechnology Project Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Biotechnology Project Manager jobs?

Cities near Riverside, CA with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $100,346 per year, or $48.2 per hour.

Medical Information Specialist

Irvine, CA • On-site

Biotechnology/Pharmaceuticals
See more jobs at Biotechnology/Pharmaceuticalsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Medical Information Specialist

We are seeking an experienced Medical Information Specialist to support global medical information activities across multiple therapeutic areas. This role is responsible for developing scientific content, responding to complex medical inquiries, evaluating clinical literature, and ensuring accurate medical communication for healthcare professionals and internal stakeholders. The ideal candidate will possess strong medical writing skills, clinical knowledge, and experience interpreting scientific data while collaborating with global cross functional teams. This position also supports international medical information operations and works closely with external service partners.

Key Responsibilities:

  • Develop, review, and maintain global medical information content and scientific response documents.
  • Respond to complex medical information inquiries from healthcare professionals and internal business partners.
  • Evaluate clinical literature, treatment guidelines, and scientific publications to develop evidence based medical responses.
  • Prepare and maintain scientific documentation and Data on File supporting medical information activities.
  • Review medical content to ensure scientific accuracy, consistency, and regulatory compliance.
  • Interpret clinical trial data and communicate scientific information to diverse audiences.
  • Collaborate with cross functional teams to develop and improve medical information resources.
  • Identify medical information trends and insights from inquiry data to support continuous improvement.
  • Support international medical information operations and collaborate with external medical information service providers.
  • Lead and participate in multidisciplinary meetings while maintaining high quality project execution.

Required Qualifications:

  • Bachelor's degree in Nursing, Pharmacy, Physician Assistant, Health Sciences, or Medical degree.
  • Experience supporting Medical Information within the pharmaceutical or biotechnology industry.
  • Strong medical writing experience.
  • Experience evaluating scientific literature and clinical research.
  • Knowledge of clinical trial methodology and statistical concepts.
  • Strong understanding of disease states, treatment guidelines, and product labeling.
  • Excellent written and verbal English communication skills.
  • Strong organizational skills with the ability to manage multiple priorities.
  • Proficiency with MS Office including Excel and PowerPoint.

Preferred Qualifications:

  • Advanced degree such as PharmD, PhD, MD, DO, or Masters degree.
  • Experience using Veeva Vault.
  • Experience using Salesforce.
  • Understanding of pharmaceutical regulatory requirements.
  • Experience supporting global medical information organizations.
  • Experience collaborating with international teams and external service providers.

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - as applicable.

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